{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88362",
      "recalling_firm": "Roche Diabetes Care, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution.",
      "recall_number": "Z-2354-2021",
      "product_description": "Accu-Chek Inform II Test Strip, Whole Blood Glucose Test System, Model number 05942891001",
      "product_quantity": "9,555,555 (US); 5,128,758 (OUS)",
      "reason_for_recall": "Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.",
      "recall_initiation_date": "20210728",
      "center_classification_date": "20210826",
      "report_date": "20210901",
      "code_info": "Since this is a labeling correction, this recall is not lot specific and is applicable to all non-expired lots."
    }
  ]
}